PMID- 34727881 OWN - NLM STAT- MEDLINE DCOM- 20211104 LR - 20240404 IS - 1471-2377 (Electronic) IS - 1471-2377 (Linking) VI - 21 IP - 1 DP - 2021 Nov 2 TI - Persistent intrathecal interleukin-8 production in a patient with SARS-CoV-2-related encephalopathy presenting aphasia: a case report. PG - 426 LID - 10.1186/s12883-021-02459-3 [doi] LID - 426 AB - BACKGROUND: Neurological manifestations of coronavirus disease 2019 (COVID-19) are increasingly recognized and include encephalopathy, although direct infection of the brain by SARS-CoV-2 remains controversial. We herein report the clinical course and cytokine profiles of a patient with severe SARS-CoV-2-related encephalopathy presenting aphasia. CASE PRESENTATION: An 81-year-old man developed acute consciousness disturbance and status epileptics several days after SARS-CoV-2 infection. Following treatment with remdesivir and dexamethasone, his consciousness and epileptic seizures improved; however, amnestic aphasia and agraphia remained. Two months after methylprednisolone pulse and intravenous immunoglobulin, his neurological deficits improved. We found increased levels of interleukin (IL)-6, IL-8, and monocyte chemoattractant protein-1 (MCP-1), but not IL-2 and IL-10 in the serum and cerebrospinal fluid (CSF), and the levels of serum IL-6 and MCP-1 were much higher than those in the CSF. The level of IL-8 in the CSF after immunotherapy was four times higher than that before immunotherapy. CONCLUSION: The cytokine profile of our patient was similar to that seen in severe SARS-CoV-2-related encephalopathy. We demonstrated (i) that the characteristic aphasia can occur as a focal neurological deficit associated with SARS-CoV-2-related encephalopathy, and (ii) that IL8-mediated central nervous system inflammation follows systemic inflammation in SARS-CoV-2-related encephalopathy and can persist and worsen even after immunotherapy. Monitoring IL-8 in CSF, and long-term corticosteroids may be required for treating SARS-CoV-2-related encephalopathy. CI - (c) 2021. The Author(s). FAU - Kudo, Takuya AU - Kudo T AD - Department of Neurology, Gifu University Graduate School of Medicine, 1-1 Yanagido, 501-1194, Gifu, Japan. FAU - Hayashi, Yuichi AU - Hayashi Y AD - Department of Neurology, Gifu University Graduate School of Medicine, 1-1 Yanagido, 501-1194, Gifu, Japan. FAU - Kunieda, Kenjiro AU - Kunieda K AD - Department of Neurology, Gifu University Graduate School of Medicine, 1-1 Yanagido, 501-1194, Gifu, Japan. FAU - Yoshikura, Nobuaki AU - Yoshikura N AD - Department of Neurology, Gifu University Graduate School of Medicine, 1-1 Yanagido, 501-1194, Gifu, Japan. FAU - Kimura, Akio AU - Kimura A AD - Department of Neurology, Gifu University Graduate School of Medicine, 1-1 Yanagido, 501-1194, Gifu, Japan. FAU - Otsuki, Mika AU - Otsuki M AD - Faculty of Health Sciences, Graduate School of Sciences, Hokkaido University, Kita 15, Nishi 7, Kitaku, 060-8638, Sapporo, Japan. FAU - Shimohata, Takayoshi AU - Shimohata T AUID- ORCID: 0000-0002-8788-9089 AD - Department of Neurology, Gifu University Graduate School of Medicine, 1-1 Yanagido, 501-1194, Gifu, Japan. shimohata@gmail.com. LA - eng PT - Case Reports PT - Journal Article DEP - 20211102 PL - England TA - BMC Neurol JT - BMC neurology JID - 100968555 RN - 0 (Interleukin-8) SB - IM MH - Aged, 80 and over MH - *Aphasia MH - *Brain Diseases MH - *COVID-19 MH - Humans MH - Interleukin-8 MH - Male MH - SARS-CoV-2 PMC - PMC8560881 OTO - NOTNLM OT - Aphasia OT - Case report OT - Encephalopathy OT - IL-8 OT - SARS-CoV-2 COIS- The authors report no disclosures relevant to the manuscript. EDAT- 2021/11/04 06:00 MHDA- 2021/11/05 06:00 PMCR- 2021/11/02 CRDT- 2021/11/03 05:36 PHST- 2021/08/11 00:00 [received] PHST- 2021/10/20 00:00 [accepted] PHST- 2021/11/03 05:36 [entrez] PHST- 2021/11/04 06:00 [pubmed] PHST- 2021/11/05 06:00 [medline] PHST- 2021/11/02 00:00 [pmc-release] AID - 10.1186/s12883-021-02459-3 [pii] AID - 2459 [pii] AID - 10.1186/s12883-021-02459-3 [doi] PST - epublish SO - BMC Neurol. 2021 Nov 2;21(1):426. doi: 10.1186/s12883-021-02459-3.